383136-44-5 Usage
Uses
Used in Organic Synthesis:
1-(2-PYRIDINYL)-1H-PYRROLE-2-CARBALDEHYDE is used as a building block in organic synthesis for the preparation of various complex molecules. Its unique structure allows it to be a key component in the creation of a wide range of organic compounds.
Used in Pharmaceutical Development:
1-(2-PYRIDINYL)-1H-PYRROLE-2-CARBALDEHYDE is utilized as a starting material in the development of new drugs due to its potential biological activities. Its pharmacological properties are being studied to explore its use in medicinal chemistry for treating various conditions.
Used in Chemical Research:
In the field of chemical research, 1-(2-PYRIDINYL)-1H-PYRROLE-2-CARBALDEHYDE serves as a valuable compound for studying the properties and reactions of heterocyclic compounds. Its reactivity and structural features make it an important subject for scientific investigation and understanding the underlying principles of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 383136-44-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,3,1,3 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 383136-44:
(8*3)+(7*8)+(6*3)+(5*1)+(4*3)+(3*6)+(2*4)+(1*4)=145
145 % 10 = 5
So 383136-44-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O/c13-8-9-4-3-7-12(9)10-5-1-2-6-11-10/h1-8H
383136-44-5Relevant academic research and scientific papers
Cationic triazinium heterocycles by intramolecular NN bond formation
Reeves, Jonathan T.,Han, Zhengxu S.,Goyal, Navneet,Lee, Heewon,Busacca, Carl A.,Senanayake, Chris H.
supporting information, p. 2492 - 2494 (2014/05/06)
Tricyclic heterocycles with a cationic triazinium core were prepared by an intramolecular NN bond forming reaction of an azine oxime precursor. The azine oxime substrates were prepared by SNAr N-arylation of 2-formylpyrroles followed by oxime formation of the formyl moiety. The synthesis was demonstrated with five different azines and several functional groups.
